Papers associated with brain (and aplnr)

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	Annexin A3 Regulates Early Blood Vessel Formation., Meadows SM., PLoS One. July 16, 2015; 10 (7): e0132580.
	Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4., Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.
	Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
	Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. January 1, 2011; 128 (7-10): 327-41.
	Claudin-like protein 24 interacts with the VEGFR-2 and VEGFR-3 pathways and regulates lymphatic vessel development., Saharinen P., Genes Dev. May 1, 2010; 24 (9): 875-80.
	Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.
	Rasip1 is required for endothelial cell motility, angiogenesis and vessel formation., Xu K., Dev Biol. May 15, 2009; 329 (2): 269-79.
	A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds., Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.
	The Wnt signaling regulator R-spondin 3 promotes angioblast and vascular development., Kazanskaya O., Development. November 1, 2008; 135 (22): 3655-64.
	A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development., Rodrigues CO., Development. June 1, 2008; 135 (11): 1903-11.
	A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
	SHP-2 is required for the maintenance of cardiac progenitors., Langdon YG., Development. November 1, 2007; 134 (22): 4119-30.
	Cloning and activation of the bullfrog apelin receptor: Gi/o coupling and high affinity for [Pro1]apelin-13., Moon MJ., Mol Cell Endocrinol. October 15, 2007; 277 (1-2): 51-60.
	Paracrine and autocrine mechanisms of apelin signaling govern embryonic and tumor angiogenesis., Kälin RE., Dev Biol. May 15, 2007; 305 (2): 599-614.
	Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.
	Apelin, the ligand for the endothelial G-protein-coupled receptor, APJ, is a potent angiogenic factor required for normal vascular development of the frog embryo., Cox CM., Dev Biol. August 1, 2006; 296 (1): 177-89.
	Embryonic expression of Xenopus laevis SOX7., Fawcett SR., Gene Expr Patterns. January 1, 2004; 4 (1): 29-33.
	Degradation of hyaluronan by a Hyal2-type hyaluronidase affects pattern formation of vitelline vessels during embryogenesis of Xenopus laevis., Müllegger J., Mech Dev. February 1, 2002; 111 (1-2): 25-35.
	The receptor tyrosine kinase EphB4 and ephrin-B ligands restrict angiogenic growth of embryonic veins in Xenopus laevis., Helbling PM., Development. January 1, 2000; 127 (2): 269-78.
	Elucidating the origins of the vascular system: a fate map of the vascular endothelial and red blood cell lineages in Xenopus laevis., Mills KR., Dev Biol. May 15, 1999; 209 (2): 352-68.
	Towards a molecular anatomy of the Xenopus pronephric kidney., Brändli AW., Int J Dev Biol. January 1, 1999; 43 (5): 381-95.
	Neovascularization of the Xenopus embryo., Cleaver O., Dev Dyn. September 1, 1997; 210 (1): 66-77.
	Expression of a new G protein-coupled receptor X-msr is associated with an endothelial lineage in Xenopus laevis., Devic E., Mech Dev. October 1, 1996; 59 (2): 129-40.

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